A 43-year-old woman was being investigated for dyspesia and had an ultrasound examination. This revealed an asymptomatic mass that appeared to involve the left kidney. Subsequent investigation established that the tumor was, in fact, intrarenal and a nephrectomy was performed. Post-operative clinical evaluation failed to disclose a neoplasm at any other site.
Gross examination of the kidney showed a solid, homogeneous, tan tumor in the hilar region measuring 2.5 cm in maximum diameter. One pericaval lymph node contained metastatic tumor. The pathologist initially examining the gross specimen thought the appearance was somewhat unusual for renal cell carcinoma and a portion was fixed in glutaraldehyde for electron microscopy. By the time histological slides were available, ultrastructural evidence of many neurosecretory granules within tumor cell cytoplasm established the neoplasm as a primary or metastatic carcinoid (Figures 1 and 2). Also present was another feature common to carcinoids, intracytopasmic accumulations of intermediate filaments. In addition, typical features of renal cell carcinoma such as lumens with microvilli, lipid vacuoles and collections of glycogen were absent. Histology as complexly interconnecting cord of tumor cells was consistent with a carcinoid tumor (Figures 3 and 4).
Primary renal carcinoid